NDC 72189-167 – Losartan Potassium And Hydrochlorothiazide

Losartan Potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC72189-167

Product details

Brand name
Losartan Potassium And Hydrochlorothiazide
Generic name
Losartan Potassium And Hydrochlorothiazide
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078245
Marketed since
January 8, 2021
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
72189-167-3030 TABLET in 1 BOTTLE (72189-167-30)Jan 8, 2021
72189-167-9090 TABLET in 1 BOTTLE (72189-167-90)Jan 8, 2021

Recalls mentioning this NDC

Other Losartan Potassium and Hydrochlorothiazide products